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HRID 1488451作成日:2026年10月27日

Acetic Acid → 4-Acetamido-2,6-dimethylanisole

https://huagongshe.com/reaction/1488451

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Acetic AnhydrideHCID 7918—
反応物Sodium BicarbonateHCID 516892—
反応物4-Methoxy-3,5-dimethylanilineHCID 4166097—
溶媒WaterHCID 962—
生成物4-Acetamido-2,6-dimethylanisoleHCID 2185276483%

反応条件

温度50 °C

反応手順

4-Amino-2,6-dimethylanisole (4, 5 g, 33.2 mmol) was placed in a round-bottom flask fitted with a reflux condenser, and acetic anhydride (3.4 mL, 35.4 mmol) and acetic acid (3 mL, 53.1 mmol) were added sequentially. The mixture was heated to 50° C. for 4 h, cooled, poured into water and basified with saturated aq. sodium bicarbonate. The solution was extracted with methylene chloride, and the combined extracts were washed with brine and dried (MgSO4). Removing the solvent and recrystallizing the resulting solid from hexane-methylene chloride yielded 4-acetamido-2,6-dimethylanisole (7, 5.3 g, 83% yield). Spectral data: 1H NMR: δ 2.1 (s, 3H), 2.2 (s, 6H), 3.65 (s, 3H), 7.10 (s, 2H), 8.10 (s, 1H); 13C NMR: δ 16.1, 24.2, 60.0, 121.5, 131.8, 134.3, 154.3, 169.8; CI-HRMS: calcd. for C11H16NO2 (M+H+) 194.1181, fnd. 194.1181.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05674876
出典データセットuspto-grants-1997_10
ORD IDord-71a403f3a8a64d90bf3e76cd93ce52c7
出典メモuspto-grants-1997_10